Variant report

Variant	nsv536559
Chromosome Location	chr3:46831085-46873527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:732)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:46871161-46871655	GM12878	blood:	n/a	n/a
2	BACH1	chr3:46853993-46854163	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr3:46871182-46871599	GM12878	blood:	n/a	n/a
4	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
5	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:46871123-46871508	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
8	BCLAF1	chr3:46871037-46871634	GM12878	blood:	n/a	n/a
9	CBX3	chr3:46864817-46865093	K562	blood:	n/a	n/a
10	CBX3	chr3:46862397-46862721	K562	blood:	n/a	n/a
11	CBX3	chr3:46862333-46862734	K562	blood:	n/a	n/a
12	CBX3	chr3:46853564-46854307	K562	blood:	n/a	n/a
13	CCNT2	chr3:46853838-46854110	K562	blood:	n/a	chr3:46854080-46854089
14	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr3:46853890-46853892	GM12878	blood:	n/a	n/a
16	CHD2	chr3:46853361-46853740	H1-hESC	embryonic stem cell:	n/a	chr3:46853514-46853524
17	CHD2	chr3:46871277-46871496	GM12878	blood:	n/a	n/a
18	CREB1	chr3:46871143-46871711	GM12878	blood:	n/a	n/a
19	CREB1	chr3:46871225-46871696	GM12878	blood:	n/a	n/a
20	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr3:46871060-46871210	GM12873	blood:	n/a	n/a
22	CTCF	chr3:46871020-46871170	GM12872	blood:	n/a	n/a
23	CTCF	chr3:46871020-46871170	K562	blood:	n/a	n/a
24	CTCF	chr3:46850120-46850270	GM12873	blood:	n/a	chr3:46850217-46850226
25	CTCF	chr3:46854325-46854386	GM20000	blood:	n/a	n/a
26	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr3:46871040-46871190	GM12873	blood:	n/a	n/a
28	CTCF	chr3:46871060-46871210	GM12864	blood:	n/a	n/a
29	CTCF	chr3:46871180-46871330	GM12870	blood:	n/a	n/a
30	CTCF	chr3:46865442-46865496	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr3:46871000-46871150	GM12864	blood:	n/a	n/a
32	CTCF	chr3:46871220-46871370	GM12864	blood:	n/a	n/a
33	CTCF	chr3:46871040-46871190	GM12875	blood:	n/a	n/a
34	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
35	CTCF	chr3:46871111-46871197	Lung_OC	lung:	n/a	n/a
36	CTCF	chr3:46850200-46850350	GM12864	blood:	n/a	chr3:46850217-46850226
37	CTCF	chr3:46853580-46853730	SAEC	small airway:	n/a	n/a
38	CTCF	chr3:46850080-46850230	GM12873	blood:	n/a	chr3:46850217-46850226
39	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
41	CTCF	chr3:46846140-46846290	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr3:46871000-46871150	GM12866	blood:	n/a	n/a
43	CTCF	chr3:46854876-46854950	GM20000	blood:	n/a	n/a
44	CTCF	chr3:46871020-46871170	GM12865	blood:	n/a	n/a
45	E2F6	chr3:46853813-46854245	A549	lung:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
46	E2F6	chr3:46852724-46853059	H1-hESC	embryonic stem cell:	n/a	n/a
47	E2F6	chr3:46853655-46854327	A549	lung:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
48	E2F6	chr3:46853178-46854309	H1-hESC	embryonic stem cell:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
49	E2F6	chr3:46852784-46853010	K562	blood:	n/a	n/a
50	E2F6	chr3:46853117-46854270	H1-hESC	embryonic stem cell:	n/a	chr3:46854080-46854089 chr3:46854114-46854124

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46854311-46854361	MCF10A-Er-Src	breast:	n/a
2	chr3:46856803-46856853	H1-hESC	embryonic stem cell:	embryo
3	chr3:46854311-46854361	K562	blood:	n/a
4	chr3:46854297-46854347	NHBE	bronchial:	n/a
5	chr3:46853850-46853900	NHDF-neo	bronchial:	n/a
6	chr3:46854297-46854347	Hela-S3	cervix:	n/a
7	chr3:46850588-46850638	T-47D	breast:	n/a
8	chr3:46853986-46854036	HEEpiC	esophagus:	n/a
9	chr3:46854297-46854347	Jurkat	blood:	n/a
10	chr3:46853986-46854036	AG10803	skin:	n/a
11	chr3:46854311-46854361	HRPEpiC	eye:	n/a
12	chr3:46854173-46854223	AG04449	skin:	fetal
13	chr3:46853631-46853681	NHBE	bronchial:	n/a
14	chr3:46854311-46854361	ovcar-3	ovarian:	n/a
15	chr3:46856803-46856853	HRCEpiC	kidney:	n/a
16	chr3:46872239-46872289	BE2_C	brain:	n/a
17	chr3:46872949-46872999	NT2-D1	testis:	n/a
18	chr3:46853910-46853960	T-47D	breast:	n/a
19	chr3:46854297-46854347	AoSMC	blood vessel:	n/a
20	chr3:46854297-46854347	HEEpiC	esophagus:	n/a
21	chr3:46853631-46853681	GM12891	blood:	n/a
22	chr3:46853986-46854036	ECC-1	luminal epithelium:	n/a
23	chr3:46872949-46872999	PFSK-1	brain:	n/a
24	chr3:46850588-46850638	GM12892	blood:	n/a
25	chr3:46854297-46854347	HL-60	blood:	n/a
26	chr3:46854311-46854361	AG09319	gingival:	n/a
27	chr3:46854311-46854361	HRCEpiC	kidney:	n/a
28	chr3:46853631-46853681	HCF	heart:	n/a
29	chr3:46854297-46854347	HCF	heart:	n/a
30	chr3:46854173-46854223	MCF-7	breast:	n/a
31	chr3:46853850-46853900	ProgFib	skin:	n/a
32	chr3:46854173-46854223	AG09319	gingival:	n/a
33	chr3:46854231-46854281	BJ	skin:	n/a
34	chr3:46854173-46854223	LNCaP	prostate:	n/a
35	chr3:46850588-46850638	HAEpiC	amniotic membrane:	n/a
36	chr3:46872949-46872999	SAEC	small airway:	n/a
37	chr3:46854297-46854347	MCF10A-Er-Src	breast:	n/a
38	chr3:46854231-46854281	HRPEpiC	eye:	n/a
39	chr3:46850588-46850638	AG04449	skin:	fetal
40	chr3:46853850-46853900	HEEpiC	esophagus:	n/a
41	chr3:46854311-46854361	HCPEpiC	choroid plexus:	n/a
42	chr3:46854231-46854281	ProgFib	skin:	n/a
43	chr3:46854311-46854361	SK-N-SH_RA	brain:	n/a
44	chr3:46853910-46853960	HMEC	breast:	n/a
45	chr3:46853986-46854036	HCT-116	colon:	n/a
46	chr3:46853986-46854036	A549	lung:	n/a
47	chr3:46854311-46854361	SK-N-MC	brain:	n/a
48	chr3:46853631-46853681	Hela-S3	cervix:	n/a
49	chr3:46854311-46854361	LNCaP	prostate:	n/a
50	chr3:46854173-46854223	GM06990	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46864966..46867284-chr3:46873787..46876389,2	K562	blood:
2	chr3:46853522..46855564-chr3:46864841..46866780,2	K562	blood:
3	chr3:46858188..46860125-chr3:46939783..46942119,2	K562	blood:
4	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46853712-46854064	NONHSAT089457
2	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458
3	lnc-PRSS42-2	chr3:46869999-46870324	NONHSAT089461
4	lnc-PRSS42-3	chr3:46869645-46869919	NONHSAT089460

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS50	TF binding region
PRSS44	TF binding region
PRSS45	TF binding region
ENSG00000238013	CpG island
PRSS50	CpG island
PRSS44	CpG island
PRSS45	CpG island
ENSG00000188086	chromatin interactions
ENSG00000178055	chromatin interactions
ENSG00000206549	chromatin interactions

Extended variants
information (count: 932 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:932 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573731003	chr3:46831131-46831132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76254953	chr3:46831191-46831192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372162784	chr3:46834796-46834797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs376771917	chr3:46834851-46834852	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs543068216	chr3:46834881-46834882	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs550625350	chr3:46834886-46834887	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs576336238	chr3:46834936-46834937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs6442034	chr3:46835016-46835017	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs150746644	chr3:46835072-46835073	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs190282658	chr3:46835076-46835077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs565377039	chr3:46835079-46835080	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs533020209	chr3:46835082-46835083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs181250794	chr3:46835106-46835107	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs138997573	chr3:46835144-46835145	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs527552896	chr3:46835234-46835235	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186760162	chr3:46835245-46835246	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs7429588	chr3:46835250-46835251	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs147211681	chr3:46835273-46835274	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs190705674	chr3:46835302-46835303	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs541023151	chr3:46835313-46835314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs181003520	chr3:46835357-46835358	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs533060006	chr3:46835362-46835363	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs183526790	chr3:46838820-46838821	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs112064679	chr3:46838841-46838842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374471828	chr3:46838848-46838849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs186667040	chr3:46839113-46839114	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs192340465	chr3:46839226-46839227	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs529788719	chr3:46839262-46839263	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs367771687	chr3:46839291-46839292	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs548813699	chr3:46839315-46839316	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs546566239	chr3:46839614-46839615	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs56059045	chr3:46839644-46839645	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs568235547	chr3:46839660-46839661	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs75114699	chr3:46839680-46839681	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs112010465	chr3:46839719-46839720	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs189982882	chr3:46839733-46839734	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs35394638	chr3:46839737-46839738	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs536844759	chr3:46839739-46839740	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs558849556	chr3:46839777-46839778	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs577043623	chr3:46839795-46839796	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs77332439	chr3:46839833-46839834	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs542214544	chr3:46844089-46844090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527757829	chr3:46844114-46844115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6779016	chr3:46844247-46844248	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs561824795	chr3:46844270-46844271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529082950	chr3:46844304-46844305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142941607	chr3:46844314-46844315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569117687	chr3:46844344-46844345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560862230	chr3:46844355-46844356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73065601	chr3:46844375-46844376	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46830800-46831200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr3:46844000-46844400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:46844000-46844400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:46844400-46847400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:46845600-46846400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:46846400-46851400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:46847800-46849600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr3:46848400-46852800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:46848600-46849200	Enhancers	Fetal Intestine Large	intestine
10	chr3:46849000-46852600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr3:46849200-46851800	Weak transcription	Fetal Intestine Large	intestine
12	chr3:46849600-46849800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr3:46849800-46850000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:46850000-46850400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr3:46850000-46850600	Enhancers	GM12878-XiMat	blood
16	chr3:46850000-46852600	Weak transcription	Right Ventricle	heart
17	chr3:46850200-46850400	Enhancers	Fetal Thymus	thymus
18	chr3:46850400-46850600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr3:46850400-46851400	Weak transcription	Fetal Thymus	thymus
20	chr3:46850400-46853200	Weak transcription	Fetal Intestine Small	intestine
21	chr3:46850600-46850800	Enhancers	Lung	lung
22	chr3:46850600-46851800	Weak transcription	GM12878-XiMat	blood
23	chr3:46850600-46852000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr3:46851000-46852200	Weak transcription	Lung	lung
25	chr3:46851000-46853600	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr3:46851400-46852000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:46851400-46852200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr3:46851400-46852200	Enhancers	Thymus	Thymus
29	chr3:46851400-46853200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:46851400-46853200	Enhancers	Fetal Thymus	thymus
31	chr3:46851800-46852000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr3:46851800-46852000	Enhancers	Fetal Intestine Large	intestine
33	chr3:46851800-46852200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr3:46851800-46852400	Enhancers	GM12878-XiMat	blood
35	chr3:46851800-46853400	Enhancers	K562	blood
36	chr3:46851800-46856800	Enhancers	Fetal Heart	heart
37	chr3:46852000-46853000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr3:46852000-46853000	Enhancers	Spleen	Spleen
39	chr3:46852000-46853200	Enhancers	Placenta Amnion	Placenta Amnion
40	chr3:46852200-46852400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr3:46852200-46852400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:46852200-46852600	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr3:46852200-46852600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr3:46852200-46852600	Active TSS	Thymus	Thymus
45	chr3:46852200-46853400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr3:46852200-46853600	Enhancers	Lung	lung
47	chr3:46852400-46852800	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr3:46852400-46853200	Weak transcription	Right Atrium	heart
49	chr3:46852400-46853800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr3:46852600-46852800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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